| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC112694767, AIFM3 (Y527C +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | AIFM3, LOC112694767 (G530S +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | AIFM3, LOC112694767 (G534R +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene